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- NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_assertion type Assertion NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_head.
- NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_provenance.
- NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_assertion evidence source_evidence_literature NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_provenance.
- NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_assertion SIO_000772 22544363 NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_provenance.
- NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_assertion wasDerivedFrom befree-2016 NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_provenance.
- NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_assertion wasGeneratedBy ECO_0000203 NP978444.RAI2vCH70z-fYIHBhfNTSllqgh_6s6_W2nLH5Eub-rafY130_provenance.